ZA201101041B - 3h-imidazo [4,5-c] pyridine-6-carboxamides as anti-inflammatory agents - Google Patents
3h-imidazo [4,5-c] pyridine-6-carboxamides as anti-inflammatory agentsInfo
- Publication number
- ZA201101041B ZA201101041B ZA2011/01041A ZA201101041A ZA201101041B ZA 201101041 B ZA201101041 B ZA 201101041B ZA 2011/01041 A ZA2011/01041 A ZA 2011/01041A ZA 201101041 A ZA201101041 A ZA 201101041A ZA 201101041 B ZA201101041 B ZA 201101041B
- Authority
- ZA
- South Africa
- Prior art keywords
- carboxamides
- imidazo
- pyridine
- inflammatory agents
- inflammatory
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/02—Nasal agents, e.g. decongestants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/04—Antipruritics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/04—Drugs for skeletal disorders for non-specific disorders of the connective tissue
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/06—Antigout agents, e.g. antihyperuricemic or uricosuric agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/06—Antimigraine agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/16—Otologicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/24—Drugs for disorders of the endocrine system of the sex hormones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/58—Benzoxazoles; Hydrogenated benzoxazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D277/82—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Gynecology & Obstetrics (AREA)
- Vascular Medicine (AREA)
- Virology (AREA)
- Emergency Medicine (AREA)
- Ophthalmology & Optometry (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US9998708P | 2008-09-25 | 2008-09-25 | |
EP08165120 | 2008-09-25 | ||
PCT/EP2009/062424 WO2010034798A1 (fr) | 2008-09-25 | 2009-09-25 | <sp>3</sp>h-imidazo[4,5-c]pyridine-6-carboxamides comme agents anti-inflammatoires |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA201101041B true ZA201101041B (en) | 2011-10-26 |
Family
ID=40344110
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA2011/01041A ZA201101041B (en) | 2008-09-25 | 2011-02-09 | 3h-imidazo [4,5-c] pyridine-6-carboxamides as anti-inflammatory agents |
ZA2011/01042A ZA201101042B (en) | 2008-09-25 | 2011-02-09 | 3h-imidazo [4,5-b] pyridine-6-carboxamides as anti-inflammatory agents |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA2011/01042A ZA201101042B (en) | 2008-09-25 | 2011-02-09 | 3h-imidazo [4,5-b] pyridine-6-carboxamides as anti-inflammatory agents |
Country Status (17)
Country | Link |
---|---|
US (4) | US8598190B2 (fr) |
EP (4) | EP2350073B1 (fr) |
JP (4) | JP5591807B2 (fr) |
KR (4) | KR20110060910A (fr) |
CN (4) | CN102164924A (fr) |
AR (4) | AR073684A1 (fr) |
AU (4) | AU2009295816A1 (fr) |
BR (3) | BRPI0919292A2 (fr) |
CA (4) | CA2737552A1 (fr) |
IL (4) | IL211138A0 (fr) |
MX (4) | MX2011002903A (fr) |
NZ (4) | NZ591846A (fr) |
RU (4) | RU2011116128A (fr) |
TW (4) | TW201016682A (fr) |
UY (1) | UY32138A (fr) |
WO (4) | WO2010034799A1 (fr) |
ZA (2) | ZA201101041B (fr) |
Families Citing this family (93)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100250458A1 (en) * | 2009-03-30 | 2010-09-30 | Mspot, Inc. | Content based social networking system and method |
UY32138A (es) | 2008-09-25 | 2010-04-30 | Boehringer Ingelheim Int | Amidas sustituidas del ácido 2-(2,6-dicloro-fenilamino)-6-fluoro-1-metil-1h-bencimidazol-5-carboxílico y sus sales farmacéuticamente aceptables |
CA2737694C (fr) * | 2008-09-26 | 2013-07-02 | Merck Sharp & Dohme Corp. | Nouveaux derives de benzimidazole cycliques utiles en tant qu'agents anti-diabetiques |
UY32470A (es) * | 2009-03-05 | 2010-10-29 | Boehringer Ingelheim Int | Derivados de 2-{2-cloro-5-[(sustituido) metil]fenilamino} -1-metil]fenilamino}-1-metilbencimidazol-5-carboxamidas-n-(sustituidas) y sus sales fisiológicamente aceptables, composiciones conteniéndolos y aplicaciones |
CA2940954A1 (fr) | 2009-05-12 | 2010-11-18 | Romark Laboratories L.C. | Nitazoxanide et tizoxanide pour le traitement des infections a rhinovirus et a rhabdovirus |
WO2010151577A1 (fr) | 2009-06-26 | 2010-12-29 | Romark Laboratories L.C. | Composés et procédés pour traiter la grippe |
WO2011099832A2 (fr) * | 2010-02-12 | 2011-08-18 | Crystalgenomics, Inc. | Nouveau composé de benzimidazole, son procédé de préparation et composition pharmaceutique le contenant |
US8759537B2 (en) * | 2010-08-20 | 2014-06-24 | Boehringer Ingelheim International Gmbh | 3H-imidazo [4, 5-C] pyridine-6-carboxamides as anti-inflammatory agents |
US8586604B2 (en) | 2010-08-20 | 2013-11-19 | Boehringer Ingelheim International Gmbh | Inhibitors of the microsomal prostaglandin E2 synthase-1 |
TW201305178A (zh) | 2010-10-29 | 2013-02-01 | Glenmark Pharmaceuticals Sa | 作為mPGES-1抑制物的三環化合物 |
US8466186B2 (en) | 2010-12-10 | 2013-06-18 | Boehringer Ingelheim International Gmbh | Compounds |
US8674113B2 (en) | 2010-12-10 | 2014-03-18 | Boehringer Ingelheim International Gmbh | Compounds |
US8486968B2 (en) | 2010-12-10 | 2013-07-16 | Boehringer Ingelheim International Gmbh | Compounds |
AR084174A1 (es) | 2010-12-21 | 2013-04-24 | Lilly Co Eli | Compuestos de imidazol-2-benzamida utiles para el tratamiento de osteoartritis y una composicion farmaceutica |
WO2012102937A2 (fr) * | 2011-01-25 | 2012-08-02 | Irm Llc | Composés qui développent des cellules souches hématopoïétiques |
MX348131B (es) * | 2011-02-25 | 2017-05-26 | Merck Sharp & Dohme | Novedosos derivados de azabencimidazol ciclico utiles como agentes antidiabeticos. |
EP2495244A1 (fr) | 2011-03-02 | 2012-09-05 | NovaSaid AB | Dérivés de piperidinyl-benzoimidazole en tant qu'inhibiteurs de mPGEs-1 |
CN103702993B (zh) * | 2011-07-18 | 2015-11-25 | 默克专利有限公司 | 苯甲酰胺 |
WO2013038308A1 (fr) | 2011-09-15 | 2013-03-21 | Glenmark Pharmaceuticals S.A. | Composés à base d'hétéroaryle bicyclique substitué capables d'inhiber mpges-1 |
WO2013072825A1 (fr) | 2011-11-16 | 2013-05-23 | Glenmark Pharmaceuticals S.A. | Dérivés de phtalazinone en tant qu'inhibiteurs de mpges-1 |
WO2013118071A1 (fr) * | 2012-02-09 | 2013-08-15 | Glenmark Pharmaceuticals S.A. | Composés bicycliques en tant qu'inhibiteurs de mpges-1 |
WO2013153535A1 (fr) | 2012-04-13 | 2013-10-17 | Glenmark Pharmaceuticals S.A. | Composés tricycliques à titre d'inhibiteurs de la mpges-1 |
CN103450329B (zh) * | 2012-05-29 | 2015-05-27 | 首都医科大学 | 3h-咪唑并吡啶-6-甲酰氨基酸苄酯、其合成、抗肿瘤活性和应用 |
US9550737B2 (en) | 2012-06-11 | 2017-01-24 | Ucb Biopharma Sprl | TNF -α modulating benzimidazoles |
TWI568722B (zh) | 2012-06-15 | 2017-02-01 | 葛蘭馬克製藥公司 | 作爲mPGES-1抑制劑之三唑酮化合物 |
CN103922999B (zh) * | 2013-01-16 | 2016-05-04 | 上海医药工业研究院 | 一种达比加群酯中间体的制备方法及中间体化合物 |
US20140221335A1 (en) * | 2013-02-06 | 2014-08-07 | Boehringer Ingelheim International Gmbh | Substituted bicyclic dihydropyrimidinones and their use as inhibitors of neutrophil elastase activity |
CN104030977B (zh) * | 2013-03-07 | 2016-05-04 | 上海医药工业研究院 | 一种达比加群酯中间体的制备方法 |
WO2014167444A1 (fr) | 2013-04-08 | 2014-10-16 | Glenmark Pharmaceuticals S.A. | Composés bicycliques substitués utilisés en tant qu'inhibiteurs de mpges-1 |
RU2673542C2 (ru) * | 2013-06-25 | 2018-11-28 | Ф. Хоффманн-Ля Рош Аг | Соединения для лечения спинальной мышечной атрофии |
CN103435554A (zh) * | 2013-09-06 | 2013-12-11 | 中国药科大学 | 2-苯氨基苯并咪唑类化合物及其用途 |
WO2015059618A1 (fr) | 2013-10-22 | 2015-04-30 | Glenmark Pharmaceuticals S.A. | Composés de pyrimidine substitués utilisés en tant qu'inhibiteurs de mpges-1 |
MX2016010474A (es) | 2014-02-11 | 2016-10-31 | Bayer Pharma AG | Benzimidazol-2-aminas como inhibidores de midh1. |
EP3105210B1 (fr) | 2014-02-11 | 2019-01-30 | Bayer Pharma Aktiengesellschaft | Benzimidazol-2-amines comme inhibiteurs de midh1 |
WO2015166398A1 (fr) * | 2014-04-30 | 2015-11-05 | Aurigene Discovery Technologies Limited | Dérivés de 3h-imidazo[4,5-b]pyridine en tant qu'inhibiteurs de dihydroororate déshydrogénase |
CN105294829B (zh) * | 2014-06-13 | 2018-07-27 | 首都医科大学 | 咪唑并吡啶-6-甲酰-氨基酸苄酯,其合成,活性及应用 |
CN105198960B (zh) * | 2014-06-13 | 2018-10-19 | 首都医科大学 | 咪唑并吡啶-6-甲酰-Met-AA-OBzl,其合成,活性和应用 |
CN105198959B (zh) * | 2014-06-13 | 2018-09-07 | 首都医科大学 | 咪唑并吡啶-6-甲酰-Met-Glu(OBzl)2,其合成,活性和应用 |
CN105315335A (zh) * | 2014-07-10 | 2016-02-10 | 首都医科大学 | 咪唑并吡啶-6-甲酰-Met-Gln-OBzl,其合成,活性和应用 |
CN105315325A (zh) * | 2014-07-10 | 2016-02-10 | 首都医科大学 | 咪唑并吡啶-6-甲酰-Met-Arg(NO2)-OBzl,其合成,活性和应用 |
CN105254709A (zh) * | 2014-07-10 | 2016-01-20 | 首都医科大学 | 咪唑并吡啶-6-甲酰-Met-AA-OBzl,其合成,活性和应用 |
DK3174535T3 (da) | 2014-08-01 | 2019-05-13 | Glenmark Pharmaceuticals Sa | Nanopartikelformulering, der omfatter en mpges-1-hæmmer |
JP6645695B2 (ja) * | 2014-10-14 | 2020-02-14 | 中尾 洋一 | イミダゾピリジンアミン化合物、その製造方法及び用途 |
ES2814151T3 (es) | 2014-10-23 | 2021-03-26 | Deutsches Krebsforschungszentrum Stiftung Des Oeffentlichen Rechts | 1-Ciclohexilo-2-fenilaminobenzimidazoles como inhibidores de MIDH1 para el tratamiento de tumores |
ES2822654T3 (es) * | 2014-10-23 | 2021-05-04 | Deutsches Krebsforschungszentrum Stiftung Des Oeffentlichen Rechts | Benzimidazol-2-aminas como inhibidores de mIDH1 |
CN106146615B (zh) * | 2015-03-23 | 2021-08-24 | 首都医科大学 | 咪唑并吡啶-6-甲酰-氨基酸苄酯,其合成,活性和应用 |
CN107849015B (zh) | 2015-05-21 | 2021-03-19 | 葛兰素知识产权发展有限公司 | 作为pad4抑制剂的苯并咪唑衍生物 |
WO2016198322A1 (fr) | 2015-06-08 | 2016-12-15 | Bayer Pharma Aktiengesellschaft | N-menthylbenzimidazoles à titre d'inhibiteurs de midh1 |
CN107698660B (zh) * | 2015-06-23 | 2021-06-08 | 首都医科大学 | 咪唑并吡啶-6-甲酰-Lys(Lys)-寡肽,其合成,活性和应用 |
US10414734B2 (en) | 2015-07-16 | 2019-09-17 | Bayer Pharma Aktiengesellschaft | 5-hydroxyalkylbenzimidazoles as mIDH1 inhibitors |
EP3390387B1 (fr) | 2015-12-18 | 2021-11-17 | Bayer Pharma Aktiengesellschaft | Composés hétéroarylbenzimidazole |
WO2017207534A1 (fr) | 2016-06-03 | 2017-12-07 | Bayer Pharma Aktiengesellschaft | Composés hétéroarylbenzimidazole substitués |
PL3713564T3 (pl) | 2017-11-22 | 2024-04-08 | Khondrion Ip B.V. | Związki jako inhibitory mPGES-1 |
CN110294751B (zh) * | 2018-03-21 | 2020-11-20 | 湖南化工研究院有限公司 | 具生物活性的咪唑[4,5-b]并吡啶类化合物及其制备方法和应用 |
CA3142513A1 (fr) | 2019-06-25 | 2020-12-30 | Gilead Sciences, Inc. | Proteines de fusion flt3l-fc et procedes d'utilisation |
CN118178645A (zh) | 2019-10-18 | 2024-06-14 | 四十七公司 | 用于治疗骨髓增生异常综合征和急性髓系白血病的联合疗法 |
CN114599392A (zh) | 2019-10-31 | 2022-06-07 | 四十七公司 | 基于抗cd47和抗cd20的血癌治疗 |
TWI778443B (zh) | 2019-11-12 | 2022-09-21 | 美商基利科學股份有限公司 | Mcl1抑制劑 |
FI4081305T3 (fi) | 2019-12-24 | 2024-11-01 | Carna Biosciences Inc | Diasyyliglyserolikinaasia moduloivia yhdisteitä |
TW202140002A (zh) | 2020-01-20 | 2021-11-01 | 美商健臻公司 | 用於復發型多發性硬化症的治療性酪胺酸激酶抑制劑 |
PE20231067A1 (es) | 2020-02-14 | 2023-07-17 | Jounce Therapeutics Inc | Anticuerpos y proteinas de fusion que se unen a ccr8 y usos de estos |
WO2021222522A1 (fr) | 2020-05-01 | 2021-11-04 | Gilead Sciences, Inc. | Composés de 2,4-dioxopyrimidine inhibant cd73 |
US11691963B2 (en) | 2020-05-06 | 2023-07-04 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as JAK2 inhibitors |
CN114249694A (zh) * | 2020-09-22 | 2022-03-29 | 浙江四维医药科技有限公司 | 一种特格拉赞中间体的制备方法 |
CN118434732A (zh) | 2020-12-10 | 2024-08-02 | 建新公司 | Tolebrutinib的晶型及其制备方法和用途 |
EP4267574A1 (fr) | 2020-12-23 | 2023-11-01 | Ajax Therapeutics, Inc. | 6-hétéroaryloxy benzimidazoles et azabenzimidazoles utilisés en tant qu'inhibiteurs de jak2 |
TW202302145A (zh) | 2021-04-14 | 2023-01-16 | 美商基利科學股份有限公司 | CD47/SIRPα結合及NEDD8活化酶E1調節次單元之共抑制以用於治療癌症 |
TW202313094A (zh) | 2021-05-18 | 2023-04-01 | 美商基利科學股份有限公司 | 使用FLT3L—Fc融合蛋白之方法 |
US11976072B2 (en) | 2021-06-23 | 2024-05-07 | Gilead Sciences, Inc. | Diacylglycerol kinase modulating compounds |
CN117377671A (zh) | 2021-06-23 | 2024-01-09 | 吉利德科学公司 | 二酰基甘油激酶调节化合物 |
KR20240005901A (ko) | 2021-06-23 | 2024-01-12 | 길리애드 사이언시즈, 인코포레이티드 | 디아실글리세롤 키나제 조절 화합물 |
EP4359389A1 (fr) | 2021-06-23 | 2024-05-01 | Gilead Sciences, Inc. | Composés de modulation de la diacylglycérol kinase |
CN118201941A (zh) | 2021-10-29 | 2024-06-14 | 吉利德科学公司 | Cd73化合物 |
WO2023086319A1 (fr) | 2021-11-09 | 2023-05-19 | Ajax Therapeutics, Inc. | 6-hetero-aryloxy-benzimidazoles et azabenzimidazoles en tant qu'inhibiteurs de jak2 |
US12162881B2 (en) | 2021-11-09 | 2024-12-10 | Ajax Therapeutics, Inc. | Forms and compositions of inhibitors of JAK2 |
JP2024546851A (ja) | 2021-12-22 | 2024-12-26 | ギリアード サイエンシーズ, インコーポレイテッド | Ikarosジンクフィンガーファミリー分解剤及びその使用 |
EP4452415A1 (fr) | 2021-12-22 | 2024-10-30 | Gilead Sciences, Inc. | Agents de dégradation des doigts de zinc de la famille ikaros et leurs utilisations |
TW202340168A (zh) | 2022-01-28 | 2023-10-16 | 美商基利科學股份有限公司 | Parp7抑制劑 |
HRP20241457T1 (hr) | 2022-03-17 | 2025-01-03 | Gilead Sciences, Inc. | Sredstva za degradaciju porodice cinkovih prstiju ikaros i njihova uporaba |
CN119031937A (zh) | 2022-03-24 | 2024-11-26 | 吉利德科学公司 | 用于治疗表达Trop-2的癌症的联合疗法 |
TW202345901A (zh) | 2022-04-05 | 2023-12-01 | 美商基利科學股份有限公司 | 用於治療結腸直腸癌之組合療法 |
WO2023205719A1 (fr) | 2022-04-21 | 2023-10-26 | Gilead Sciences, Inc. | Composés modulateurs de kras g12d |
AU2023298558A1 (en) | 2022-07-01 | 2024-12-19 | Gilead Sciences, Inc. | Cd73 compounds |
WO2024028893A1 (fr) * | 2022-08-01 | 2024-02-08 | Council Of Scientific And Industrial Research An Indian Registered Body Incorporated Under The Regn. Of Soc. Act (Act Xxi Of 1860) | Benzimidazoles substitués pour le traitement de maladies virales |
US20240091351A1 (en) | 2022-09-21 | 2024-03-21 | Gilead Sciences, Inc. | FOCAL IONIZING RADIATION AND CD47/SIRPa DISRUPTION ANTICANCER COMBINATION THERAPY |
US20240254118A1 (en) | 2022-12-22 | 2024-08-01 | Gilead Sciences, Inc. | Prmt5 inhibitors and uses thereof |
CN116332779A (zh) * | 2023-03-13 | 2023-06-27 | 苏州敬业医药化工有限公司 | 一种3,4-二氨基苯甲酸甲酯的制备方法 |
WO2024190888A1 (fr) * | 2023-03-16 | 2024-09-19 | サンメディカル株式会社 | Kit de polymérisation dentaire |
US20240383922A1 (en) | 2023-04-11 | 2024-11-21 | Gilead Sciences, Inc. | KRAS Modulating Compounds |
WO2024220917A1 (fr) | 2023-04-21 | 2024-10-24 | Gilead Sciences, Inc. | Inhibiteurs de prmt5 et leurs utilisations |
WO2025006720A1 (fr) | 2023-06-30 | 2025-01-02 | Gilead Sciences, Inc. | Composés modulateurs de kras |
WO2025024811A1 (fr) | 2023-07-26 | 2025-01-30 | Gilead Sciences, Inc. | Inhibiteurs de parp7 |
WO2025024663A1 (fr) | 2023-07-26 | 2025-01-30 | Gilead Sciences, Inc. | Inhibiteurs de parp7 |
Family Cites Families (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3006671A1 (de) | 1980-02-22 | 1981-08-27 | Dr. Karl Thomae Gmbh, 7950 Biberach | Neue benzoxazole, deren herstellung und deren verwendung als arzneumittel |
FI91859C (fi) | 1987-06-17 | 1994-08-25 | Eisai Co Ltd | Analogiamenetelmä antiallergisena aineena aktiivisen bentsotiatsolijohdannaisen valmistamiseksi |
JPH06759B2 (ja) | 1989-09-22 | 1994-01-05 | ファイザー製薬株式会社 | 新規なベンゾイミダゾール化合物 |
SK2612001A3 (en) | 1998-08-26 | 2001-11-06 | Aventis Pharma Ltd | Aza-bicycles which modulate the inhibition of cell adhesion |
DK1153017T3 (da) * | 1999-02-16 | 2006-07-17 | Aventis Pharma Ltd | Bicykliske forbindelser og deres anvendelse som integrinreceptorligander |
TR200102959T2 (tr) * | 1999-04-12 | 2002-04-22 | Aventis Pharma Limited | İntegrin antagonistleri olarak ikame edilmiş bisiklik heteroaril bileşikleri |
CA2372840C (fr) | 1999-05-05 | 2008-07-22 | Aventis Pharma Limited | Composes bicycliques substitues |
US6340681B1 (en) | 1999-07-16 | 2002-01-22 | Pfizer Inc | 2-benzimidazolylamine compounds as ORL-1-receptor agonists |
DE60014130T2 (de) * | 1999-10-06 | 2006-03-09 | Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield | Heterocyclische verbindungen verwendbar als tyrosinkinase inhibitoren |
FR2833948B1 (fr) | 2001-12-21 | 2004-02-06 | Sod Conseils Rech Applic | Nouveaux derives de benzimidazole et leur utilisation en tant que medicament |
WO2003074515A1 (fr) | 2002-03-01 | 2003-09-12 | Smithkline Beecham Corporation | Diamino-pyrimidines et leurs utilisations en tant qu'inhibiteurs de l'angiogenese |
SI1499311T1 (sl) | 2002-03-29 | 2010-03-31 | Novartis Vaccines & Diagnostic | Substituirani benzazoli in njihova uporaba kot inhibitorji Raf kinaze |
US7037902B2 (en) | 2002-07-03 | 2006-05-02 | Receptron, Inc. | Affinity small molecules for the EPO receptor |
US7122665B2 (en) | 2002-10-15 | 2006-10-17 | Synta Pharmaceuticals Corp. | Heterocyclic compounds |
CA2515215A1 (fr) | 2003-02-10 | 2004-08-26 | Amgen Inc. | Ligands du recepteur vanilloide et leur utilisation dans des traitements |
FR2851563B1 (fr) | 2003-02-26 | 2005-04-22 | Sod Conseils Rech Applic | Nouveaux derives de benzimidazole et d'imidazo-pyridine et leur utilisation en tant que medicament |
US7531553B2 (en) | 2003-03-21 | 2009-05-12 | Amgen Inc. | Heterocyclic compounds and methods of use |
FR2852957B1 (fr) | 2003-03-31 | 2005-06-10 | Sod Conseils Rech Applic | Nouveaux derives d'imidazo-pyridine et leur utilisation en tant que medicament |
US7329682B2 (en) | 2003-04-03 | 2008-02-12 | Ewha University-Industry Collaboration Foundation | Method for inhibiting 5-lipoxygenase using a benzoxazole derivative |
EP1677791A4 (fr) | 2003-10-31 | 2007-08-15 | Takeda Pharmaceutical | Composes heterocycliques accoles contenant de l'azote |
GB0401334D0 (en) * | 2004-01-21 | 2004-02-25 | Novartis Ag | Organic compounds |
US7470712B2 (en) | 2004-01-21 | 2008-12-30 | Bristol-Myers Squibb Company | Amino-benzazoles as P2Y1 receptor inhibitors |
ES2321422T3 (es) | 2004-06-18 | 2009-06-05 | Biolipox Ab | Indoles utiles para el tratamiento de la inflamacion. |
US7521446B2 (en) | 2005-01-13 | 2009-04-21 | Signal Pharmaceuticals, Llc | Haloaryl substituted aminopurines, compositions thereof, and methods of treatment therewith |
US7723340B2 (en) * | 2005-01-13 | 2010-05-25 | Signal Pharmaceuticals, Llc | Haloaryl substituted aminopurines, compositions thereof, and methods of treatment therewith |
DE602005026867D1 (de) | 2005-01-19 | 2011-04-21 | Biolipox Ab | Entzündungshemmende indol-derivate |
US20100130473A1 (en) | 2005-02-25 | 2010-05-27 | Marc Geoffrey Hummersone | Compounds |
NZ561029A (en) * | 2005-03-14 | 2011-03-31 | High Point Pharmaceuticals Llc | Benzazole dervatives, compositions, and method of use as beta-secretase inhibitors |
EP1966222A2 (fr) * | 2005-11-16 | 2008-09-10 | SGX Pharmaceuticals, Inc. | Modulateurs de la proteine kinase a base de pyrazolothiazole |
WO2007095124A2 (fr) * | 2006-02-10 | 2007-08-23 | Transtech Pharma, Inc. | Derives, compositions de benzazole et procedes d'utilisation en tant qu'inhibiteurs de la kinase aurora |
US20070287344A1 (en) * | 2006-06-12 | 2007-12-13 | Hiroshi Ohara | Fabric Construction Specifically For Damper |
WO2008009924A2 (fr) | 2006-07-18 | 2008-01-24 | Biolipox Ab | Indoles utiles dans le traitement de l'inflammation |
KR20080027191A (ko) | 2006-09-22 | 2008-03-26 | 이화여자대학교 산학협력단 | 신규한 벤즈옥사졸 유도체, 이의 제조방법 및 이를포함하는 약학 조성물 |
EP2102177A1 (fr) | 2006-12-14 | 2009-09-23 | Boehringer Ingelheim International GmbH | Benzoxasoles utiles dans le traitement de l'inflammation |
WO2008129276A1 (fr) | 2007-04-19 | 2008-10-30 | Boehringer Ingelheim International Gmbh | Disulfonamides utiles dans le traitement de l'inflammation |
UY32138A (es) | 2008-09-25 | 2010-04-30 | Boehringer Ingelheim Int | Amidas sustituidas del ácido 2-(2,6-dicloro-fenilamino)-6-fluoro-1-metil-1h-bencimidazol-5-carboxílico y sus sales farmacéuticamente aceptables |
UY32470A (es) | 2009-03-05 | 2010-10-29 | Boehringer Ingelheim Int | Derivados de 2-{2-cloro-5-[(sustituido) metil]fenilamino} -1-metil]fenilamino}-1-metilbencimidazol-5-carboxamidas-n-(sustituidas) y sus sales fisiológicamente aceptables, composiciones conteniéndolos y aplicaciones |
US8586604B2 (en) * | 2010-08-20 | 2013-11-19 | Boehringer Ingelheim International Gmbh | Inhibitors of the microsomal prostaglandin E2 synthase-1 |
US8759537B2 (en) | 2010-08-20 | 2014-06-24 | Boehringer Ingelheim International Gmbh | 3H-imidazo [4, 5-C] pyridine-6-carboxamides as anti-inflammatory agents |
US8674113B2 (en) | 2010-12-10 | 2014-03-18 | Boehringer Ingelheim International Gmbh | Compounds |
US8466186B2 (en) | 2010-12-10 | 2013-06-18 | Boehringer Ingelheim International Gmbh | Compounds |
US8486968B2 (en) * | 2010-12-10 | 2013-07-16 | Boehringer Ingelheim International Gmbh | Compounds |
-
2009
- 2009-09-24 UY UY0001032138A patent/UY32138A/es not_active Application Discontinuation
- 2009-09-25 NZ NZ591846A patent/NZ591846A/xx not_active IP Right Cessation
- 2009-09-25 BR BRPI0919292A patent/BRPI0919292A2/pt not_active IP Right Cessation
- 2009-09-25 CA CA2737552A patent/CA2737552A1/fr not_active Abandoned
- 2009-09-25 CA CA2738083A patent/CA2738083A1/fr not_active Abandoned
- 2009-09-25 WO PCT/EP2009/062425 patent/WO2010034799A1/fr active Application Filing
- 2009-09-25 KR KR1020117006846A patent/KR20110060910A/ko not_active Application Discontinuation
- 2009-09-25 EP EP09783406.3A patent/EP2350073B1/fr not_active Not-in-force
- 2009-09-25 US US13/119,832 patent/US8598190B2/en not_active Expired - Fee Related
- 2009-09-25 US US13/119,834 patent/US8916599B2/en not_active Expired - Fee Related
- 2009-09-25 RU RU2011116128/04A patent/RU2011116128A/ru not_active Application Discontinuation
- 2009-09-25 AR ARP090103703A patent/AR073684A1/es unknown
- 2009-09-25 BR BRPI0919738A patent/BRPI0919738A2/pt not_active IP Right Cessation
- 2009-09-25 EP EP09783402A patent/EP2334652A1/fr not_active Withdrawn
- 2009-09-25 JP JP2011528330A patent/JP5591807B2/ja not_active Expired - Fee Related
- 2009-09-25 KR KR1020117006974A patent/KR20110065478A/ko not_active Application Discontinuation
- 2009-09-25 MX MX2011002903A patent/MX2011002903A/es active IP Right Grant
- 2009-09-25 CN CN2009801376014A patent/CN102164924A/zh active Pending
- 2009-09-25 CA CA2737839A patent/CA2737839A1/fr not_active Abandoned
- 2009-09-25 RU RU2011116129/04A patent/RU2011116129A/ru not_active Application Discontinuation
- 2009-09-25 MX MX2011003094A patent/MX2011003094A/es not_active Application Discontinuation
- 2009-09-25 JP JP2011528332A patent/JP5342646B2/ja not_active Expired - Fee Related
- 2009-09-25 US US13/119,835 patent/US9040565B2/en not_active Expired - Fee Related
- 2009-09-25 AU AU2009295816A patent/AU2009295816A1/en not_active Abandoned
- 2009-09-25 AR ARP090103704A patent/AR073685A1/es unknown
- 2009-09-25 AR ARP090103705A patent/AR073686A1/es unknown
- 2009-09-25 EP EP09783405A patent/EP2361252A1/fr not_active Withdrawn
- 2009-09-25 KR KR1020117006845A patent/KR20110056530A/ko not_active Application Discontinuation
- 2009-09-25 RU RU2011116131/04A patent/RU2011116131A/ru not_active Application Discontinuation
- 2009-09-25 AR ARP090103706A patent/AR073403A1/es unknown
- 2009-09-25 AU AU2009295815A patent/AU2009295815A1/en not_active Abandoned
- 2009-09-25 TW TW098132575A patent/TW201016682A/zh unknown
- 2009-09-25 CN CN2009801371627A patent/CN102164922A/zh active Pending
- 2009-09-25 NZ NZ591845A patent/NZ591845A/xx not_active IP Right Cessation
- 2009-09-25 WO PCT/EP2009/062422 patent/WO2010034797A1/fr active Application Filing
- 2009-09-25 CN CN2009801469428A patent/CN102224143A/zh active Pending
- 2009-09-25 KR KR1020117006971A patent/KR20110056533A/ko not_active Application Discontinuation
- 2009-09-25 AU AU2009295813A patent/AU2009295813A1/en not_active Abandoned
- 2009-09-25 BR BRPI0919295A patent/BRPI0919295A2/pt not_active IP Right Cessation
- 2009-09-25 TW TW098132551A patent/TW201018669A/zh unknown
- 2009-09-25 CN CN2009801376052A patent/CN102164911A/zh active Pending
- 2009-09-25 WO PCT/EP2009/062424 patent/WO2010034798A1/fr active Application Filing
- 2009-09-25 MX MX2011002948A patent/MX2011002948A/es active IP Right Grant
- 2009-09-25 NZ NZ591843A patent/NZ591843A/xx not_active IP Right Cessation
- 2009-09-25 NZ NZ591847A patent/NZ591847A/xx not_active IP Right Cessation
- 2009-09-25 AU AU2009295814A patent/AU2009295814A1/en not_active Abandoned
- 2009-09-25 RU RU2011116133/04A patent/RU2011116133A/ru not_active Application Discontinuation
- 2009-09-25 TW TW098132581A patent/TW201018684A/zh unknown
- 2009-09-25 JP JP2011528331A patent/JP5591808B2/ja not_active Expired - Fee Related
- 2009-09-25 TW TW098132579A patent/TW201016696A/zh unknown
- 2009-09-25 MX MX2011003152A patent/MX2011003152A/es active IP Right Grant
- 2009-09-25 JP JP2011528333A patent/JP5342647B2/ja not_active Expired - Fee Related
- 2009-09-25 CA CA2737384A patent/CA2737384A1/fr not_active Abandoned
- 2009-09-25 EP EP09783403A patent/EP2334664A1/fr not_active Withdrawn
- 2009-09-25 US US13/119,836 patent/US8703796B2/en not_active Expired - Fee Related
- 2009-09-25 WO PCT/EP2009/062421 patent/WO2010034796A1/fr active Application Filing
-
2011
- 2011-02-09 IL IL211138A patent/IL211138A0/en unknown
- 2011-02-09 IL IL211137A patent/IL211137A0/en unknown
- 2011-02-09 ZA ZA2011/01041A patent/ZA201101041B/en unknown
- 2011-02-09 ZA ZA2011/01042A patent/ZA201101042B/en unknown
- 2011-02-10 IL IL211148A patent/IL211148A0/en unknown
- 2011-02-10 IL IL211147A patent/IL211147A0/en unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
IL211148A0 (en) | 3h-imidazo [4,5-c] pyridine-6-carboxamides as anti-inflammatory agents | |
IL214033A0 (en) | 3h-imidazo[4,5-c]pyridine-6-caboxamides as anti-inflammatory agents | |
IL206330A (en) | Pyrido [3,2– b] pyrazine compounds maintained in position 8 as anti-proliferative agents | |
BRPI0919948A2 (pt) | Pirido[4,3-b]indois contendo porções rígidas | |
ZA201002013B (en) | BICYCLIC y-AMINO ACID DERIVATIVES | |
ZA201002334B (en) | Imidazo | |
EP2142542A4 (fr) | Nouveaux composés d'imidazo [4,5-b] pyridine-7-carboxamides 704 | |
ZA201107350B (en) | Imidazo [2 1 b] [1, 3, 4] thiadiazole derivatives | |
IL229993A (en) | 8 - Alkoxy [1,2,4] triazolo [5,1 – c] pyrimidine– 2 | |
ZA201206630B (en) | Hetaryl-[1,8]naphthyridine derivatives | |
GB0702259D0 (en) | 7-azaindole derivatives | |
IL210171A0 (en) | Substituted pyrimido[2,1-a]isoquinolin-4-one derivatives | |
HK1142323A1 (en) | 6-phenyl-1h-imidazo[4,5-c]pyridine-4-carbonitrile derivatives as cathepsin inhibitors | |
HRP20130641T1 (en) | Pyridin-2-yl derivatives as immunomodulating agents | |
ZA201101861B (en) | Compositions with and process for methylmorpholin-substituted pyrido [2,3-d] pyrimidines | |
IL216794A0 (en) | 3-substituted-8-substituted-3h imidazo[5,1-d][1,2,3,5]tetrazin-4-one compounds and their use | |
GB0702265D0 (en) | 7-Azaindole derivatives | |
IL206666A0 (en) | N-PHENYLIMIDAZO[1,2-a]PYRIDINE-2- | |
IL206668A0 (en) | N-PHENYLIMIDAZO[1,2-a]PYRIDINE-2- | |
EP2651937B8 (fr) | Dérivé imidazo[4,5-c]quinolin-1-yle utile en thérapie | |
GB0702260D0 (en) | 7-azaindole derivatives |